ClinVar Miner

Submissions for variant NM_007294.3(BRCA1):c.212+13G>A (rs752088834)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000441672 SCV000522485 likely benign not specified 2016-08-29 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Invitae RCV000464719 SCV000560316 likely benign not provided 2018-05-06 criteria provided, single submitter clinical testing
Color RCV000581548 SCV000688366 likely benign Hereditary cancer-predisposing syndrome 2017-09-11 criteria provided, single submitter clinical testing

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